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A single dose of the SARS-CoV-2 vaccine BNT162b2 elicits Fc-mediated antibody effector functions and T cell responses
While the standard regimen of the BNT162b2 mRNA vaccine for SARS-CoV-2 includes two doses administered 3 weeks apart, some public health authorities are spacing these doses, raising concerns about efficacy. However, data indicate that a single dose can be up to 90% effective starting 14 days post-ad...
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Published in: | Cell host & microbe 2021-07, Vol.29 (7), p.1137-1150.e6 |
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creator | Tauzin, Alexandra Nayrac, Manon Benlarbi, Mehdi Gong, Shang Yu Gasser, Romain Beaudoin-Bussières, Guillaume Brassard, Nathalie Laumaea, Annemarie Vézina, Dani Prévost, Jérémie Anand, Sai Priya Bourassa, Catherine Gendron-Lepage, Gabrielle Medjahed, Halima Goyette, Guillaume Niessl, Julia Tastet, Olivier Gokool, Laurie Morrisseau, Chantal Arlotto, Pascale Stamatatos, Leonidas McGuire, Andrew T. Larochelle, Catherine Uchil, Pradeep Lu, Maolin Mothes, Walther De Serres, Gaston Moreira, Sandrine Roger, Michel Richard, Jonathan Martel-Laferrière, Valérie Duerr, Ralf Tremblay, Cécile Kaufmann, Daniel E. Finzi, Andrés |
description | While the standard regimen of the BNT162b2 mRNA vaccine for SARS-CoV-2 includes two doses administered 3 weeks apart, some public health authorities are spacing these doses, raising concerns about efficacy. However, data indicate that a single dose can be up to 90% effective starting 14 days post-administration. To assess the mechanisms contributing to protection, we analyzed humoral and T cell responses three weeks after a single BNT162b2 dose. We observed weak neutralizing activity elicited in SARS-CoV-2 naive individuals but strong anti-receptor binding domain and spike antibodies with Fc-mediated effector functions and cellular CD4+ T cell responses. In previously infected individuals, a single dose boosted all humoral and T cell responses, with strong correlations between T helper and antibody immunity. Our results highlight the potential role of Fc-mediated effector functions and T cell responses in vaccine efficacy. They also provide support for spacing doses to vaccinate more individuals in conditions of vaccine scarcity.
[Display omitted]
•Three weeks after the first BNT162b2 dose, weak neutralizing antibodies are elicited•These antibodies have robust Fc-mediated effector functions•Vaccination of individuals previously infected boosts humoral and cellular responses•Strong correlations between T helper cell and humoral responses are observed
Tauzin and Nayrac et al. characterize humoral and cellular responses 3 weeks after a single dose of mRNA BNT162b2 vaccine. They show, in SARS-CoV-2-naive individuals, that the antibodies elicited have weak neutralizing activity but potent Fc-mediated effector functions, and in SARS-CoV-2 previously infected individuals, that all responses are significantly boosted. |
doi_str_mv | 10.1016/j.chom.2021.06.001 |
format | article |
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[Display omitted]
•Three weeks after the first BNT162b2 dose, weak neutralizing antibodies are elicited•These antibodies have robust Fc-mediated effector functions•Vaccination of individuals previously infected boosts humoral and cellular responses•Strong correlations between T helper cell and humoral responses are observed
Tauzin and Nayrac et al. characterize humoral and cellular responses 3 weeks after a single dose of mRNA BNT162b2 vaccine. They show, in SARS-CoV-2-naive individuals, that the antibodies elicited have weak neutralizing activity but potent Fc-mediated effector functions, and in SARS-CoV-2 previously infected individuals, that all responses are significantly boosted.</description><identifier>ISSN: 1931-3128</identifier><identifier>EISSN: 1934-6069</identifier><identifier>DOI: 10.1016/j.chom.2021.06.001</identifier><identifier>PMID: 34133950</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>ADCC ; Adult ; Antibodies, Neutralizing - immunology ; Antibodies, Viral - chemistry ; Antibodies, Viral - immunology ; Betacoronavirus ; BNT162 Vaccine ; Carrier Proteins ; coronavirus ; COVID-19 ; COVID-19 - immunology ; COVID-19 - prevention & control ; COVID-19 Vaccines - administration & dosage ; COVID-19 Vaccines - immunology ; Female ; Humans ; humoral responses ; Immunity ; Immunoglobulin Fc Fragments ; Male ; Middle Aged ; mRNA vaccine ; mRNA Vaccines ; neutralization ; SARS-CoV-2 ; SARS-CoV-2 - immunology ; spike glycoproteins ; T cell responses ; T-Lymphocytes - immunology ; Vaccination ; Vaccines, Synthetic - immunology ; variants ; Young Adult</subject><ispartof>Cell host & microbe, 2021-07, Vol.29 (7), p.1137-1150.e6</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><rights>2021 Elsevier Inc. 2021 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-78960da93cb2be20b635cc20c532b92de0295b7740b16dbc1c406c055a1240e73</citedby><cites>FETCH-LOGICAL-c455t-78960da93cb2be20b635cc20c532b92de0295b7740b16dbc1c406c055a1240e73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34133950$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tauzin, Alexandra</creatorcontrib><creatorcontrib>Nayrac, Manon</creatorcontrib><creatorcontrib>Benlarbi, Mehdi</creatorcontrib><creatorcontrib>Gong, Shang Yu</creatorcontrib><creatorcontrib>Gasser, Romain</creatorcontrib><creatorcontrib>Beaudoin-Bussières, Guillaume</creatorcontrib><creatorcontrib>Brassard, Nathalie</creatorcontrib><creatorcontrib>Laumaea, Annemarie</creatorcontrib><creatorcontrib>Vézina, Dani</creatorcontrib><creatorcontrib>Prévost, Jérémie</creatorcontrib><creatorcontrib>Anand, Sai Priya</creatorcontrib><creatorcontrib>Bourassa, Catherine</creatorcontrib><creatorcontrib>Gendron-Lepage, Gabrielle</creatorcontrib><creatorcontrib>Medjahed, Halima</creatorcontrib><creatorcontrib>Goyette, Guillaume</creatorcontrib><creatorcontrib>Niessl, Julia</creatorcontrib><creatorcontrib>Tastet, Olivier</creatorcontrib><creatorcontrib>Gokool, Laurie</creatorcontrib><creatorcontrib>Morrisseau, Chantal</creatorcontrib><creatorcontrib>Arlotto, Pascale</creatorcontrib><creatorcontrib>Stamatatos, Leonidas</creatorcontrib><creatorcontrib>McGuire, Andrew T.</creatorcontrib><creatorcontrib>Larochelle, Catherine</creatorcontrib><creatorcontrib>Uchil, Pradeep</creatorcontrib><creatorcontrib>Lu, Maolin</creatorcontrib><creatorcontrib>Mothes, Walther</creatorcontrib><creatorcontrib>De Serres, Gaston</creatorcontrib><creatorcontrib>Moreira, Sandrine</creatorcontrib><creatorcontrib>Roger, Michel</creatorcontrib><creatorcontrib>Richard, Jonathan</creatorcontrib><creatorcontrib>Martel-Laferrière, Valérie</creatorcontrib><creatorcontrib>Duerr, Ralf</creatorcontrib><creatorcontrib>Tremblay, Cécile</creatorcontrib><creatorcontrib>Kaufmann, Daniel E.</creatorcontrib><creatorcontrib>Finzi, Andrés</creatorcontrib><title>A single dose of the SARS-CoV-2 vaccine BNT162b2 elicits Fc-mediated antibody effector functions and T cell responses</title><title>Cell host & microbe</title><addtitle>Cell Host Microbe</addtitle><description>While the standard regimen of the BNT162b2 mRNA vaccine for SARS-CoV-2 includes two doses administered 3 weeks apart, some public health authorities are spacing these doses, raising concerns about efficacy. However, data indicate that a single dose can be up to 90% effective starting 14 days post-administration. To assess the mechanisms contributing to protection, we analyzed humoral and T cell responses three weeks after a single BNT162b2 dose. We observed weak neutralizing activity elicited in SARS-CoV-2 naive individuals but strong anti-receptor binding domain and spike antibodies with Fc-mediated effector functions and cellular CD4+ T cell responses. In previously infected individuals, a single dose boosted all humoral and T cell responses, with strong correlations between T helper and antibody immunity. Our results highlight the potential role of Fc-mediated effector functions and T cell responses in vaccine efficacy. They also provide support for spacing doses to vaccinate more individuals in conditions of vaccine scarcity.
[Display omitted]
•Three weeks after the first BNT162b2 dose, weak neutralizing antibodies are elicited•These antibodies have robust Fc-mediated effector functions•Vaccination of individuals previously infected boosts humoral and cellular responses•Strong correlations between T helper cell and humoral responses are observed
Tauzin and Nayrac et al. characterize humoral and cellular responses 3 weeks after a single dose of mRNA BNT162b2 vaccine. They show, in SARS-CoV-2-naive individuals, that the antibodies elicited have weak neutralizing activity but potent Fc-mediated effector functions, and in SARS-CoV-2 previously infected individuals, that all responses are significantly boosted.</description><subject>ADCC</subject><subject>Adult</subject><subject>Antibodies, Neutralizing - immunology</subject><subject>Antibodies, Viral - chemistry</subject><subject>Antibodies, Viral - immunology</subject><subject>Betacoronavirus</subject><subject>BNT162 Vaccine</subject><subject>Carrier Proteins</subject><subject>coronavirus</subject><subject>COVID-19</subject><subject>COVID-19 - immunology</subject><subject>COVID-19 - prevention & control</subject><subject>COVID-19 Vaccines - administration & dosage</subject><subject>COVID-19 Vaccines - immunology</subject><subject>Female</subject><subject>Humans</subject><subject>humoral responses</subject><subject>Immunity</subject><subject>Immunoglobulin Fc Fragments</subject><subject>Male</subject><subject>Middle Aged</subject><subject>mRNA vaccine</subject><subject>mRNA Vaccines</subject><subject>neutralization</subject><subject>SARS-CoV-2</subject><subject>SARS-CoV-2 - immunology</subject><subject>spike glycoproteins</subject><subject>T cell responses</subject><subject>T-Lymphocytes - immunology</subject><subject>Vaccination</subject><subject>Vaccines, Synthetic - immunology</subject><subject>variants</subject><subject>Young Adult</subject><issn>1931-3128</issn><issn>1934-6069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kcFuEzEQhlcIREvhBTggH7nsMrbX3qyEkEJEoVIFEg1cLXt2tnG0WQd7E6lv02fpk-GQtoILJ1uef37P_F9RvOZQceD63brCVdhUAgSvQFcA_ElxyltZlxp0-_TPnZeSi9lJ8SKlNYBS0PDnxYmsuZStgtNiP2fJj9cDsS4kYqFn04rY1fz7VbkIP0vB9hbRj8Q-fl1yLZxgNHj0U2LnWG6o83aijtlx8i50N4z6nnAKkfW7EScfxpRrHVve3SINA4uUtvmN0sviWW-HRK_uz7Pix_mn5eJLefnt88VifllirdRUNrNWQ2dbiU44EuC0VIgCUEnhWtERiFa5pqnBcd055FiDxrym5aIGauRZ8eHou925PC3SOEU7mG30GxtvTLDe_FsZ_cpch72Z8UZpobLB23uDGH7tKE1m49NhFztS2CUjVC1kjnsms1QcpRhDSpH6x284mAMwszYHYOYAzIA2GVhuevP3gI8tD4Sy4P1RQDmmvadoEnoaMUcfc9SmC_5__r8BqN-ngw</recordid><startdate>20210714</startdate><enddate>20210714</enddate><creator>Tauzin, Alexandra</creator><creator>Nayrac, Manon</creator><creator>Benlarbi, Mehdi</creator><creator>Gong, Shang Yu</creator><creator>Gasser, Romain</creator><creator>Beaudoin-Bussières, Guillaume</creator><creator>Brassard, Nathalie</creator><creator>Laumaea, Annemarie</creator><creator>Vézina, Dani</creator><creator>Prévost, Jérémie</creator><creator>Anand, Sai Priya</creator><creator>Bourassa, Catherine</creator><creator>Gendron-Lepage, Gabrielle</creator><creator>Medjahed, Halima</creator><creator>Goyette, Guillaume</creator><creator>Niessl, Julia</creator><creator>Tastet, Olivier</creator><creator>Gokool, Laurie</creator><creator>Morrisseau, Chantal</creator><creator>Arlotto, Pascale</creator><creator>Stamatatos, Leonidas</creator><creator>McGuire, Andrew T.</creator><creator>Larochelle, Catherine</creator><creator>Uchil, Pradeep</creator><creator>Lu, Maolin</creator><creator>Mothes, Walther</creator><creator>De Serres, Gaston</creator><creator>Moreira, Sandrine</creator><creator>Roger, Michel</creator><creator>Richard, Jonathan</creator><creator>Martel-Laferrière, Valérie</creator><creator>Duerr, Ralf</creator><creator>Tremblay, Cécile</creator><creator>Kaufmann, Daniel E.</creator><creator>Finzi, Andrés</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210714</creationdate><title>A single dose of the SARS-CoV-2 vaccine BNT162b2 elicits Fc-mediated antibody effector functions and T cell responses</title><author>Tauzin, Alexandra ; Nayrac, Manon ; Benlarbi, Mehdi ; Gong, Shang Yu ; Gasser, Romain ; Beaudoin-Bussières, Guillaume ; Brassard, Nathalie ; Laumaea, Annemarie ; Vézina, Dani ; Prévost, Jérémie ; Anand, Sai Priya ; Bourassa, Catherine ; Gendron-Lepage, Gabrielle ; Medjahed, Halima ; Goyette, Guillaume ; Niessl, Julia ; Tastet, Olivier ; Gokool, Laurie ; Morrisseau, Chantal ; Arlotto, Pascale ; Stamatatos, Leonidas ; McGuire, Andrew T. ; Larochelle, Catherine ; Uchil, Pradeep ; Lu, Maolin ; Mothes, Walther ; De Serres, Gaston ; Moreira, Sandrine ; Roger, Michel ; Richard, Jonathan ; Martel-Laferrière, Valérie ; Duerr, Ralf ; Tremblay, Cécile ; Kaufmann, Daniel E. ; Finzi, Andrés</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-78960da93cb2be20b635cc20c532b92de0295b7740b16dbc1c406c055a1240e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>ADCC</topic><topic>Adult</topic><topic>Antibodies, Neutralizing - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell host & microbe</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tauzin, Alexandra</au><au>Nayrac, Manon</au><au>Benlarbi, Mehdi</au><au>Gong, Shang Yu</au><au>Gasser, Romain</au><au>Beaudoin-Bussières, Guillaume</au><au>Brassard, Nathalie</au><au>Laumaea, Annemarie</au><au>Vézina, Dani</au><au>Prévost, Jérémie</au><au>Anand, Sai Priya</au><au>Bourassa, Catherine</au><au>Gendron-Lepage, Gabrielle</au><au>Medjahed, Halima</au><au>Goyette, Guillaume</au><au>Niessl, Julia</au><au>Tastet, Olivier</au><au>Gokool, Laurie</au><au>Morrisseau, Chantal</au><au>Arlotto, Pascale</au><au>Stamatatos, Leonidas</au><au>McGuire, Andrew T.</au><au>Larochelle, Catherine</au><au>Uchil, Pradeep</au><au>Lu, Maolin</au><au>Mothes, Walther</au><au>De Serres, Gaston</au><au>Moreira, Sandrine</au><au>Roger, Michel</au><au>Richard, Jonathan</au><au>Martel-Laferrière, Valérie</au><au>Duerr, Ralf</au><au>Tremblay, Cécile</au><au>Kaufmann, Daniel E.</au><au>Finzi, Andrés</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A single dose of the SARS-CoV-2 vaccine BNT162b2 elicits Fc-mediated antibody effector functions and T cell responses</atitle><jtitle>Cell host & microbe</jtitle><addtitle>Cell Host Microbe</addtitle><date>2021-07-14</date><risdate>2021</risdate><volume>29</volume><issue>7</issue><spage>1137</spage><epage>1150.e6</epage><pages>1137-1150.e6</pages><issn>1931-3128</issn><eissn>1934-6069</eissn><abstract>While the standard regimen of the BNT162b2 mRNA vaccine for SARS-CoV-2 includes two doses administered 3 weeks apart, some public health authorities are spacing these doses, raising concerns about efficacy. However, data indicate that a single dose can be up to 90% effective starting 14 days post-administration. To assess the mechanisms contributing to protection, we analyzed humoral and T cell responses three weeks after a single BNT162b2 dose. We observed weak neutralizing activity elicited in SARS-CoV-2 naive individuals but strong anti-receptor binding domain and spike antibodies with Fc-mediated effector functions and cellular CD4+ T cell responses. In previously infected individuals, a single dose boosted all humoral and T cell responses, with strong correlations between T helper and antibody immunity. Our results highlight the potential role of Fc-mediated effector functions and T cell responses in vaccine efficacy. They also provide support for spacing doses to vaccinate more individuals in conditions of vaccine scarcity.
[Display omitted]
•Three weeks after the first BNT162b2 dose, weak neutralizing antibodies are elicited•These antibodies have robust Fc-mediated effector functions•Vaccination of individuals previously infected boosts humoral and cellular responses•Strong correlations between T helper cell and humoral responses are observed
Tauzin and Nayrac et al. characterize humoral and cellular responses 3 weeks after a single dose of mRNA BNT162b2 vaccine. They show, in SARS-CoV-2-naive individuals, that the antibodies elicited have weak neutralizing activity but potent Fc-mediated effector functions, and in SARS-CoV-2 previously infected individuals, that all responses are significantly boosted.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34133950</pmid><doi>10.1016/j.chom.2021.06.001</doi><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1931-3128 |
ispartof | Cell host & microbe, 2021-07, Vol.29 (7), p.1137-1150.e6 |
issn | 1931-3128 1934-6069 |
language | eng |
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source | BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS |
subjects | ADCC Adult Antibodies, Neutralizing - immunology Antibodies, Viral - chemistry Antibodies, Viral - immunology Betacoronavirus BNT162 Vaccine Carrier Proteins coronavirus COVID-19 COVID-19 - immunology COVID-19 - prevention & control COVID-19 Vaccines - administration & dosage COVID-19 Vaccines - immunology Female Humans humoral responses Immunity Immunoglobulin Fc Fragments Male Middle Aged mRNA vaccine mRNA Vaccines neutralization SARS-CoV-2 SARS-CoV-2 - immunology spike glycoproteins T cell responses T-Lymphocytes - immunology Vaccination Vaccines, Synthetic - immunology variants Young Adult |
title | A single dose of the SARS-CoV-2 vaccine BNT162b2 elicits Fc-mediated antibody effector functions and T cell responses |
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